Design of polydactyl zinc-finger proteins for unique addressing within complex genomes

被引:224
作者
Liu, Q
Segal, DJ
Ghiara, JB
Barbas, CF
机构
[1] Scripps Res Inst, DEPT MOL BIOL, LA JOLLA, CA 92037 USA
[2] SCRIPPS RES INST, SKAGGS INST CHEM BIOL, LA JOLLA, CA 92037 USA
关键词
molecule design; zinc-finger proteins; genome addressing; transcriptional regulation; gene therapy;
D O I
10.1073/pnas.94.11.5525
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Zinc-finger proteins of the Cys(2)-His(2) type represent a class of malleable DNA-binding proteins that may be selected to bind diverse sequences, Typically, zinc-finger proteins containing three zinc-finger domains, like the murine transcription factor Zif268 and the human transcription factor Sp1, bind nine contiguous base pairs, To create a class of proteins that would be generally applicable to target unique sites within complex genomes, we have utilized structure-based modeling to design a polypeptide linker that fuses two three-finger proteins, Two six-fingered proteins were created and demonstrated to bind 18 contiguous bp of DNA in a sequence-specific fashion, Expression of these proteins as fusions to activation or repression domains allows transcription to be specifically up- or down-modulated within human cells, Polydactyl zinc-finger proteins should be broadly applicable as genome-specific transcriptional switches in gene therapy strategies and the development of novel transgenic plants and animals.
引用
收藏
页码:5525 / 5530
页数:6
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